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Lichen planopilaris and pseudopelade of Brocq involve distinct disease associated gene expression patterns by microarray

  • Mei Yu

      Affiliations

    • Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
    • Vancouver Coastal Health Research Institute, Vancouver, Canada
  • ,
  • Robert H. Bell

      Affiliations

    • Prostate Centre, Vancouver General Hospital, Vancouver, Canada
  • ,
  • Elizabeth K. Ross

      Affiliations

    • Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
  • ,
  • Blanche K.K. Lo

      Affiliations

    • Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
  • ,
  • Megan Isaac-Renton

      Affiliations

    • Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
  • ,
  • Magda Martinka

      Affiliations

    • Department of Pathology, University of British Columbia, Vancouver, Canada
  • ,
  • Anne Haegert

      Affiliations

    • Prostate Centre, Vancouver General Hospital, Vancouver, Canada
  • ,
  • Jerry Shapiro

      Affiliations

    • Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
  • ,
  • Kevin J. McElwee

      Affiliations

    • Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
    • Vancouver Coastal Health Research Institute, Vancouver, Canada
    • Corresponding Author InformationCorresponding author at: Department of Dermatology and Skin Science, University of British Columbia, 835 W. 10th Ave., Vancouver, BC V5Z 1L8, Canada. Tel.: +1 604 875 4747; fax: +1 604 875 9919.

Received 2 April 2009; received in revised form 19 October 2009; accepted 22 October 2009. published online 12 July 2010.
Corrected Proof

Abstract 

Background

Lichen planopilaris (LPP) and pseudopelade of Brocq (PPB) are two scarring alopecia diagnoses that exhibit similar clinical features. Some suggest LPP and PPB are not distinct diseases, but rather different clinical presentations in a spectrum derived from the same underlying pathogenic mechanism.

Objective

We explored the degree of similarity between LPP and PPB gene expression patterns and the potential for common and unique gene pathway and gene activity in LPP and PPB using microarrays.

Methods

Microarray analysis, using a 21K cDNA set, was performed on pairs of biopsies obtained from affected and unaffected scalp of untreated patients. Diagnosis was confirmed by histopathology. Significantly differentially expressed genes were identified by analysis of microarray results in various datasets and screened for signaling pathway involvement. Selected genes were validated by quantitative PCR and immunohistology.

Results

The global gene expression profiles in LPP and PPB versus comparative intra-control scalp tissue were distinguishable by significance analysis of microarrays (SAM). There was limited commonality in the gene expression profiles between LPP and PPB. Specific genes, such as MMP11, TNFSF13B, and APOL2, were identified with significantly differential expression in association with LPP versus PPB.

Conclusions

Our findings may have important implications for understanding the pathogenesis of LPP and PPB at the molecular level. Results suggest LPP and PPB involve different mechanisms of disease development and should be regarded as biologically distinct cicatricial alopecia diagnoses. Genes that we have identified may be useful as markers of the respective diagnoses and may be potential therapeutic targets.

Abbreviations: APOL2, apolipoprotein L2, FDR, false discovery rate, GO, Gene Ontology, LPP, lichen planopilaris, MMP11, matrix metallopeptidase 11, PPB, pseudopelade of Brocq, qPCR, quantitative reverse transcriptase PCR, TNFSF13B, tumor necrosis factor (ligand) superfamily, member 13b

Keywords: Lichen planopilaris, Pseudopelade of Brocq, Cicatricial alopecia, Microarray

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PII: S0923-1811(09)00304-1

doi:10.1016/j.jdermsci.2009.10.011

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